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Leptospira

*Leptospira interrogans*

For medical students2 min readUpdated 2026-10-10

Leptospira are motile, helical bacteria that cause leptospirosis, an acute zoonotic infection. The infection is characterized by severe damage to capillaries, the liver, kidneys, and central nervous system, leading to undulating fever and hemorrhagic syndrome.

Obligate AerobesStrict aerobes that utilize lipids as their energy source.
Dark-Field MicroscopyPoorly Gram-stained, thus studied using dark-field microscopy.
RodentsThe primary natural reservoir of infection is mice and rats, which shed bacteria in their urine.
HemorrhagesThe pathogen destroys capillary walls, causing multiple hemorrhages in organs.

Morphology and Staining Properties

The causative agent of leptospirosis (L. interrogans) belongs to the family Leptospiraceae. They are thin spirochetes, 6–24 µm in length and no more than 0.15 µm in diameter.

Cultural Properties and Resistance

Leptospires are aerobes and grow slowly. The optimal temperature for their multiplication is 28–30 °C, which is lower than normal human body temperature.

Lipids—long-chain fatty acids and alcohols—serve as their energy and carbon source. Cultivation on artificial media strictly requires the addition of serum albumin or blood serum. In liquid media, they multiply by transverse fission, without causing turbidity (growth remains transparent).

Environmental Resistance:

FactorEffect on Leptospires
Drying and low pHRapidly killed
HeatDestroyed at 56 °C in 25–30 minutes, instantly upon boiling
Wet environment (water bodies)Remain viable for up to 30 days
Moist soilCan survive long-term—up to 280 days

Epidemiology and Pathogenesis

Leptospirosis is a natural focal zoonosis with a characteristic summer-autumn seasonality. Wild and synanthropic rodents serve as the primary reservoir, while domestic animals (dogs, pigs, cattle) act as secondary reservoirs. In animals, the infection proceeds chronically and asymptomatically: bacteria are shed in urine, contaminating soil and water.

Humans are highly susceptible but represent a "dead end" for the infection—the pathogen is practically never transmitted from a sick person to a healthy one.

Phases of Infection Development:

  1. Portal of entry: Intact mucous membranes of the gastrointestinal tract or skin microtraumas (waterborne transmission predominates).
  2. Primary dissemination: Penetration into the bloodstream and seeding of organs of the reticuloendothelial system (kidneys, liver).
  3. Incubation period: Lasts 7–10 days; bacteria actively multiply in parenchymal organs.
  4. Secondary bacteremia: Massive release of leptospires and their toxins into the blood, which coincides with the acute onset of clinical manifestations.
  5. Organopathology: Bacteria damage capillaries, causing hemorrhagic syndrome, jaundice, aseptic meningitis, and renal failure. Case fatality rates range from 3% to 40%.

Diagnosis, Treatment, and Prevention

Biological samples for laboratory testing (blood, urine, cerebrospinal fluid, serum) are chosen depending on the stage of the disease.

Treatment: The basis of etiotropic therapy is antibiotics of the penicillin and tetracycline groups. Additionally, specific heterologous antileptospiral immunoglobulin, derived from equine serum, is used.

Prevention: Nonspecific measures include rodent control (deratization) and the vaccination of farm animals. For epidemiological indications, specific prophylaxis in humans is carried out using a heat-killed whole-cell vaccine containing antigens of the four main serogroups.

Frequently asked questions

What virulence factors do leptospires possess?

Leptospiral virulence factors include endotoxins, exotoxin-like substances, and various aggressins.

  • Endotoxin — A lipopolysaccharide (LPS) complex with low endotoxic activity, possessing pyogenic, dermonecrotic, and lethal properties.
  • Exotoxin-like substances — Possess cytotoxic and hemolytic properties (cytotoxins, hemolysins).
  • Aggressins — Fibrinolysin, plasmocoagulase, lipase, paraoxonase, collagenase, and phospholipase C.
What biological material is collected from a patient to diagnose leptospirosis in the first and second weeks of the disease?

The choice of biological material for diagnosing leptospirosis depends on the stage of the infectious process.

  • First week of illness — Citrated blood is collected for testing.
  • From the second week of illness — Urine is analyzed.
  • In meningitis — Cerebrospinal fluid (CSF) is examined.
What species of Leptospira are distinguished in modern classification besides the pathogenic L. interrogans?

In modern taxonomy, saprophytic leptospires are distinguished alongside the pathogenic species.

  • Pathogenic species (L. interrogans) — Parasitic microorganisms causing disease in humans and animals.
  • Saprophytic species (L. biflexa) — Free-living microorganisms inhabiting the external environment (soil and water). This species includes over 60 serovars.
How do humans contract leptospirosis?

The main route of transmission is waterborne, through swimming in contaminated water bodies or consuming contaminated water. Alimentarily and contact routes are also possible.

Can you contract leptospirosis from an infected person?

No. Despite the fact that humans are highly susceptible to the pathogen and shed it into the environment, they represent an epidemiological "dead end" and do not serve as a source of infection for other people.

Is immunity developed after recovering from the infection?

Yes, durable humoral immunity is established. However, it is strictly serovar-specific—protecting only against the specific strain of bacteria that caused the disease.

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